|
Geothermometry: isotope
|
Geothermometry: SiO2 phases
|
Heat flow - 2m probes
|
5
|
- Multiple isotope systems (hydrogen, carbon, oxygen, and/or sulphur) provide narrowly constrained temperature.
- Analytical quality of results can be shown to be high (based on standards measured, sample replication, and calibration logs).
- Steam and water discharge are both collected without air contamination.
|
- Corrections for the following effects:
- pH effects on silica solubility when pH > 9.
- Salinity effects corrected for waters higher than seawater
- Mixing /dilution effects with other sources (groundwater or surface)
- Precipitation losses after sampling
- Concentrations plotted against enthalpy to confirm
- Appropriate phase selection: (<180 °C, chalcedony or quartz; 200 - 300 °C, quartz)
- Analytical quality of results can be shown to be high (based on standards measured, sample replication, and calibration logs).
|
- Reconnaissance completed in ordered grids and transects across known faults and/or other structural features.
- Use of high-quality probe (such as thermocouple) with measurements of instrument error.
- Use in areas where the groundwater aquifer is not above the geothermal system.
- Results with significant standard deviations (outliers) eliminated prior to extrapolation to equilibrium.
|
4
|
- Some, but not all of multiple isotope systems (hydrogen, carbon, oxygen, and/or sulphur) provide similar temperatures .
- Corrections can be made for mixing /dilution effects with other water sources (groundwater or surface) - particularly relevant for oxidation of H2S.
|
- All of the data correction best practices listed above.
- Not plotted against enthalpy
- Appropriate phase selection: (<180 °C, chalcedony or quartz; 200 - 300 °C, quartz)
|
- Reconnaissance completed in either ordered grids or transects across faults.
- Use of standard quality probes (thermistor or thermocouple) with measurements of instrument error.
- Use in areas where the groundwater aquifer location has not been determined in respect to the geothermal system.
|
3
|
- Multiple isotope systems (hydrogen, carbon, oxygen, and/or sulphur) provide narrowly constrained temperature.
- Mixing /dilution effects with other water sources are not well understood or corrected for.
- Steam and water discharge are not separated completely, or have evidence of air contamination.
|
- Not enough information available to implement data correction best practices (e.g. erroneous pH, not enough information to identify dissolved silica or proportion of steam separated).
- Significant, unexplained differences in sample results.
- Not plotted against enthalpy.
- Possibly inappropriate phase selection: (chalcedony at near or >180 °C, or quartz at near or >300 °C).
|
- Use in areas where groundwater aquifer overlies the geothermal system.
- Incomplete penetration due to sediment stiffness or unconsolidation.
- Minimal probes placed without consideration of underlying geology.
- Samples taken after likely reservoir dilution/mixing (i.e. spring snow melt, recent irrigation) and extrapolated to depth.
|
2
|
- Results taken from previous third-party studies of the area (either literature or contractors) with little or limited information on survey methods, replication, or error.
|
1
|
- Assumed from studies of analogous geothermal settings, or extrapolated from studies of nearby areas.
|